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GeneQ17927869· pop 6· linked from 378 articles

Also known as HBGF-4, HST, HST-1, HSTF1, K-FGF, KFGF, fibroblast growth factor 4, HSTF-1

Fibroblast growth factor 4 is a protein that in humans is encoded by the FGF4 gene.

Gene data

FGF4
Name
fibroblast growth factor 4
Type
protein-coding
Position
69,771,022–69,775,341 (−)
Aliases
FGF-4, HBGF-4, HST, HST-1, HSTF-1, HSTF1, K-FGF, KFGF, SRTD22
RefSeq RNA
NM_002007.4
RefSeq protein
NP_001998.1

The protein encoded by this gene is a member of the fibroblast growth factor (FGF) family. FGF family members possess broad mitogenic and cell survival activities and are involved in a variety of biological processes including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth and invasion. This gene was identified by its oncogenic transforming activity. This gene and FGF3, another oncogenic growth factor, are located closely on chromosome 11. Co-amplification of both genes was found in various kinds of human tumors. Studies on the mouse homolog suggested a function in bone morphogenesis and limb development through the sonic hedgehog (SHH) signaling pathway. [provided by RefSeq, Jul 2008].

via MyGene.info

Gene · Ensembl

fibroblast growth factor 4

Symbol
FGF4
Biotype
Protein coding
Organism
Homo sapiens
Location
11:69,771,022-69,775,344
Strand
Reverse (−)
Assembly
GRCh38
View on Ensembl →

via Ensembl · EMBL-EBI

Wikidata facts

Image
Protein FGF4 PDB 1ijt.png
Show 5 more facts
HomoloGene ID
1522
genomic end
69775341
genomic start
69771022
cytogenetic location
11q13.3
Sources (4)

via Wikidata · CC0

~3 min read

Article

4 sections
Contents
  • Function
  • Clinical significance
  • References
  • Further reading

Fibroblast growth factor 4 is a protein that in humans is encoded by the FGF4 gene.

The protein encoded by this gene is a member of the fibroblast growth factor (FGF) family. FGF family members possess broad mitogenic and cell survival activities and are involved in a variety of biological processes including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth and invasion. This gene was identified by its oncogenic transforming activity. This gene and FGF3, another oncogenic growth factor, are located closely on chromosome 11. Co-amplification of both genes was found in various kinds of human tumors. Studies on the mouse homolog suggested a function in bone morphogenesis and limb development through the sonic hedgehog (SHH) signaling pathway.

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